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Neuromuscular Channelopathies Panel

Test Information

Title
Neuromuscular Channelopathies Panel
Category
Neurogenetics
Test Name (CMS Title)
Neuromuscular Disease
Gene/Platform/Region List
ATP1A2, CACNA1A, CACNA1S, CLCN1, KCNA1, KCNE3, KCNJ2, SCN4A, SLC12A3
Test type
Samples Accepted
Blood, DNA
Indications
Carrier Cascade Testing, Diagnosis
Test Methodology
Sequencing
Disease/Condition
Neuromuscular Channelopathies, myotonia congenita, paramyotonia congenita, hyperkalemic periodic paralysis, hypokalemic periodic paralysis, Andersen-Tawil syndrome, potassium-aggravated myotonia

Last Updated: December 09, 2025